Stretchable conductive nanofibers, stretchable electrode using the same and method of producing the stretchable conductive nanofibers

ABSTRACT

A method of producing stretchable conductive nanofibers includes: providing stretchable nanofibers; providing a metal precursor solution by dissolving metal precursors in a solvent that may swell the stretchable nanofibers; bringing the stretchable nanofibers into contact with the metal precursor solution or its vapor for a sufficient time for the metal precursors to penetrate into the stretchable nanofibers; and reduce the metal precursors inside the stretchable nanofibers to metal nanoparticles.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of Korean Patent Application No.10-2011-0079715, filed on Aug. 10, 2011, in the Korean IntellectualProperty Office, the disclosure of which is incorporated herein in itsentirety by reference.

BACKGROUND

1. Field

The present disclosure relates to stretchable conductive compositenanofibers, a stretchable electrode using the same and methods ofproducing the stretchable conductive nanofibers.

2. Description of the Related Art

Fiber-based electronic devices have many advantages that make themdesirable to replace various electronic devices currently available inconsumer markets. For example, fiber-based electronic devices areexpected to have improved and excellent tensile strength and weavabilityproperties, large surface areas, and variety of surface treatments, andeasy formation of composites. Examples of fiber-based electronic devicesmay include textile solar cells, stretchable transistors, stretchabledisplays, exterior-stimulated drug delivery, biosensors and gas sensors,light-controlling functional textiles, functional armor clothing, andother functional armor products, etc.

In the field of micro-electronic devices having flexibility andelasticity, it is important to develop electrodes that are stretchablewhile maintaining conductivity. Materials such as metals have goodconductivity, but they are rigid and stiff, and it is difficult to use ametal as it is. When materials such as carbon nanotubes or graphenes areused on their own, it is also difficult to make stretchable electrodes.

Fibrous electrodes as stretchable electrodes and methods of producing aconductive percolation network on the surface of fibers to implementfibrous electrodes have been studied. However, when the conductivepercolation network is formed only on the surface of the fibers, thereis a limit imposed on a range of strain magnitude where the fibrouselectrodes can endure while maintaining conductivity and its percolationnetwork.

SUMMARY

Provided are stretchable conductive nanofibers which have internalconductivity to maintain conductivity under high strain environment andmethods of preparing the same.

Provided are stretchable electrodes composed of stretchable conductivenanofibers which have internal conductivity to maintain conductivityduring a high strain process.

Additional aspects will be set forth in part in the description whichfollows and, in part, will be apparent from the description, or may belearned by practice of the presented embodiments.

According to an aspect of the present invention, a stretchableconductive nanofiber includes stretchable nanofibers and a percolationnetwork of conductive nanoparticles formed inside the stretchablenanofibers. According to an embodiment, a stretchable nanofibercontaining conductive nanoparticles formed inside the nanofiber whichendows the nanofiber with conductivity is sometimes called as“stretchable conductive composite nanofiber” for convenience. Thus, inan exemplary embodiment, a stretchable conductive composite nanofiberincludes a stretchable polymeric nanofiber; and a conductivenanoparticles formed inside the stretchable polymeric nanofiber, saidnanoparticles forming a percolation structure inside the nanofiber. Thestretchable conductive composite nanofiber may further containconductive nanoparticles disposed on a surface of the nanofiber. Thestretchable conductive composite nanofiber may form a mat formed ofplural nanofibers, and the resulting mat may further contain apercolation structure formed of conductive nanoparticles in a spaceinside the mat and nanoparticles bound to a surface of individualstretchable composite nanofibers.

According to another aspect of the present invention, a stretchableconductive electrode includes stretchable conductive nanofibers.

According to another aspect of the present invention, a method ofproducing stretchable conductive nanofibers includes forming stretchablenanofibers; preparing a solution of metal precursors by dissolving metalprecursors in a solvent that may swell the stretchable nanofibers;immersing the stretchable nanofibers in the solution of metal precursorsto swell the stretchable nanofibers, so the metal precursors maypenetrate inside the stretchable nanofibers and disperse; removing anddrying the stretchable nanofibers from the solution of metal precursors;and reducing the metal precursors that have penetrated inside thestretchable nanofibers to metal nanoparticles.

In still another aspect, a method of producing the stretchableconductive nanofibers includes providing stretchable nanofibers;providing a metal precursor solution by dissolving metal precursors in asolvent that may swell the stretchable nanofibers; bringing thestretchable nanofibers into contact with the metal precursor solutionfor a sufficient time for the metal precursors to penetrate into thestretchable nanofibers; and reduce the metal precursors inside thestretchable nanofibers to metal nanoparticles.

BRIEF DESCRIPTION OF THE DRAWINGS

These and/or other aspects will become apparent and more readilyappreciated from the following description of the embodiments, taken inconjunction with the accompanying drawings of which:

FIG. 1 is a perspective view conceptually showing stretchable conductivenanofibers according to an embodiment, and FIG. 1B is a cross-sectionalview of FIG. 1A;

FIG. 2 is a flowchart illustrating a method of producing stretchableconductive nanofibers, according to an embodiment;

FIG. 3A is a scanning electron microscope (SEM) image showing apoly(styrene-butadiene-styrene)(PS-b-PB-b-PS) (SBS) nanofiber mat formedby electrospinning, and FIG. 3B is an enlarged image of a SBS nanofiberin the mat of FIG. 3A;

FIG. 4A is a SEM image of a surface of the SBS nanofiber mat after beingimmersed in the STA solution, removed, and dried. FIG. 4B is an enlargedSEM image of a portion of the surface of FIG. 4A;

FIG. 5A is a cross section image of SBS nanofibers of a stretchableconductive SBS nanofiber mat, and FIG. 5B is an enlarged transmissionelectron microscopy (TEM) image of a portion of the cross section ofFIG. 5A;

FIG. 6 is a graph showing a swelling ratio of a SBS nanofiber matimmersed in silver trifluoroacetate (STA) solution according to a STAconcentration in ethanol;

FIG. 7 is a graph showing Fourier Transform Infrared Spectroscopy(FT-IR) analysis of a SBS nanofiber mat immersed in a STA solution;

FIG. 8 is a graph showing surface resistance measurements according tothe number of strain exerted on a conductive SBS nanofiber mat;

FIG. 9A and FIG. 9B are images showing a circuit connection before andafter straining exerted on a SBS nanofiber mat in a light bulb circuitusing the SBS nanofiber mat as electrodes; and

FIG. 10 is a graph showing a current-voltage characteristic according toa strain ratio of a conductive SBS nanofiber mat.

DETAILED DESCRIPTION

Reference will now be made in detail to embodiments, examples of whichare illustrated in the accompanying drawings, wherein like referencenumerals refer to like elements throughout. In this regard, the presentembodiments may have different forms and should not be construed asbeing limited to the descriptions set forth herein. Accordingly, theembodiments are merely described below, by referring to the figures, toexplain aspects of the present description.

FIG. 1A is a perspective view conceptually showing stretchableconductive nanofibers 10 according to an embodiment, and FIG. 1B is asectional view of the conductive nanofibers 10. With reference to FIG.1A and FIG. 1B, the stretchable conductive nanofibers 10 have conductiveparticles 12 which form a percolation network inside the stretchablenanofibers 11. The percolation network includes a network formed by unitconductive particles or elements arranged and connected to each other inany direction.

The stretchable nanofibers 11 may include, for example, stretchablepolymer materials. The stretchable polymer materials may includesynthetic rubbers or natural rubbers. Examples of synthetic rubbers maybe polybutadiene (PB), poly(styrene-butadiene) (either PS-b-PB (blockpolymer of PS and PB) or PS-co-PB (copolymer of S and B)),poly(styrene-butadiene-styrene) (PS-b-PB-b-PS) (block copolymer of PS,PB and PS) (sometimes referred to as “SBS”),poly(styrene-ethylene-butylene-styrene) (SEBS), ethylene prolylene dienerubber (EPDM), acrylic rubber, polychloroprene rubber (CR), polyurethane(PU), florine rubber or butyl rubber. Examples of natural rubbers may bepolyisoprene.

The term “nanofiber” used herein indicates a fiber of a diameter rangingfrom about 10 nm to about 5.0 μm In an embodiment, the nanofiber may bea synthetic polymeric fiber, which can be prepared by a known method,such as electrospinning, and may have a diameter of about 10 nm-about5.0 μm. In an embodiment, an electrospun nanofiber may have a diameterfrom about 100 nm to about 5.0 μm.

The term “stretchable” used herein indicates that a material, e.g.,fiber is capable of extended in a direction where an external force isapplied. In the application, the word “stretchable nanofiber(s)” and“stretchable conductive nanofiber(s)” are sometimes simply referred toas “nanofiber(s)” for brevity.

The conductive nanoparticles 12 may include nanoparticles of metal orconductive metal oxide. The metal nanoparticles may include, forexample, gold, silver, copper, palladium or platinum. In an embodiment,the total mass of the conductive nanoparticles 12 may be in a range ofabout 30 to about 70 parts by weight based on total 100 parts by weightof the stretchable conductive nanofibers 10. The conductivenanoparticles 12 may have an average dimension ranging from about 5 toabout 100 nm.

Additionally, the conductive nanoparticles 12 may be formed on thesurface of the stretchable nanofibers 11. Here, the layer of theconductive nanoparticles 12 on the surface of the stretchable nanofibers11 may have a thickness in a range of about 5 to about 500 nm. Theconductive nanoparticles 12 are dispersed and form a percolation networkinside the stretchable nanofiber 11. Thus, when the stretchablenanofibers 11 are strained, an interface fracture of the percolationnetwork in the conductive nanoparticles 12 does not occur, therebymaintaining electric conductivity pathways. Therefore, conductivity isexcellent even when the stretchable conductive nanofibers 10 arerepeatedly stretched.

The term “mat” used herein indicates a flat piece of a material, e.g.,nanofibers, and may be used interchangeably with other similar termssuch as “sheet,” “film,” or “layer.” A mat of the stretchable conductivenanofibers 10 may be formed by aggregation of plural nanofibers.

FIG. 2 is a flowchart illustrating a method of producing stretchableconductive nanofibers 10, according to an embodiment.

With reference to FIG. 2, stretchable nanofibers 11 are formed (S110).The stretchable nanofibers 11 may be formed by an electrospinning methodusing stretchable polymer materials. The morphology and diameter ofstretchable nanofibers 11 during electrospinning may vary depending onfactors such as a molecular weight of a polymer, a type of a solvent, anapplied voltage, a spinning distance, a spinning temperature, spinninghumidity, and etc. Mechanical, electrical and optical properties ofnanofibers may vary depending on intrinsic properties and chemicalstructures of base materials. One skilled in the art would be able tochoose the conditions of electrospining depending on the type ofpolymeric materials as well as the usage of the resulting conductivenanofibers.

As polymers capable of forming stretchable nanofibers 11, syntheticrubbers such as polybutadiene (PB), poly(styrene-butadiene) (PS-b-PB,PS-co-PB), poly(styrene-butadiene-styrene) (PS-b-PB-b-PS) (SBS),poly(styrene-ethylene-butylene-styrene) (SEBS), ethylene prolylene dienerubber (EPDM), acrylic rubber, polychloroprene rubber (CR), polyurethane(PU), florine rubber or butyl rubber and natural rubbers such aspolyisoprene may be used. Since the above-mentioned synthetic or naturalrubbers have not been cured, the resulting nanofibers may have higherstretchability as compared to cured polymers such aspoly(dimethylsiloxane) (PDMS).

As a solvent in which these polymers are dissolved to form a polymersolution having a suitable viscosity, for example, chloroform,chlorobenzene, toluene, dimethylformaldehyde, tetrahydrofuran (THF),dimethyl sulfoxide, N-methylpyrrolidone, or fluorinert™.

In an embodiment, chloromethane, trifluoroacetic acid, dimethylacetamide, dichloromethane, 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP),acetone, isopropyl alcohol, sulphuric acid, formic acid, water, or amixture of these solvents may be used.

Methods other than electrospinning, such as wet spinning, conjugatedspinning, melt blown spinning or flash spinning may be alternativelyused.

A precursor solution of conductive material is prepared (S120). Metalmay be used as the conductive material, and for metal precursors, forexample, AgNO₃, AgCl, HAuCl₄, CuCl₂, PtCl₂ or PtCl₄ may be used, but arenot limited thereto. Any solvent may be used as long as the metalprecursors are dissolved, and the stretchable nanofibers 11 are swelledso the metal precursors may penetrate inside the stretchable nanofibers11. For example, water, methanol, ethanol, propanol, isopropyl alcohol,butanol, ethylene glycol, dimethylformamide (DMF), tetrahydrofuran (THF)or a mixture of more than two thereof may be used as a solvent. Thesolution of metal precursors may have a concentration in a range ofabout 30 to about 70 weight %. Such a solution of metal precursorswithin this range swell the stretchable nanofibers 11 enough so that themetal precursors may penetrate inside the stretchable nanofibers 11.

The stretchable nanofibers 11 are immersed in the solution of metalprecursors (S130). When a mat is formed using the stretchable nanofibers11, the mat of stretchable nanofibers 11 may be immersed in the solutionof metal precursors. When the stretchable nanofibers 11 are immersed inthe solution of metal precursors for enough time, they cause thestretchable nanofibers 11 to swell so the metal precursors may penetrateand be dispersed inside the stretchable nanofibers 11. The metalprecursors that penetrate and are dispersed inside the nanofibers maybecome metal seeds forming a nano metal percolation network inside thenanofiber. Also, the metal precursors may not only penetrate inside thestretchable nanofibers 11 but also be deposited on the surfaces of thestretchable nanofibers 11 by immersing the stretchable nanofibers 11 inthe solution of metal precursors.

For example, when SBS nanofibers are immersed for enough time in asolution of silver nitrate (AgNO₃) in ethanol prepared by dissolvingsilver nitrate in ethanol, the stretchable nanofibers 11 swell so silvernitrate may penetrate and be dispersed inside the SBS nanofibers, andthe silver nitrate may be deposited on the surfaces of the SBSnanofibers 11.

The stretchable nanofibers 11 are removed from the solution of metalprecursors and dried (S140). A rinsing process may optionally beperformed on the stretchable nanofibers 11 before drying.

Then, the metal precursors inside the stretchable nanofibers 11 arereduced to metal nanoparticles (S150). The reduction of the metalprecursors inside the stretchable nanofibers 11 to metal nanoparticlesmay be performed by treating the stretchable nanofibers 11 with areducing agent. For example, the stretchable nanofibers 11 having themetal precursors penetrated therein may be exposed to hydrazine (N₂H₄)vapor, dropped thereon with concentrated hydrazine, or immersed in asodium borohydride (NaBH₄) ethanol solution, so that the metalprecursors inside the stretchable nanofibers 11 may be reduced to metalnanoparticles. Here, the metal precursors on the surface of thestretchable nanofibers 11 may also be reduced to metal. Also, rinsingand drying processes may optionally be performed after treating thestretchable nanofibers 11 with a reducing agent.

Moreover, the metal nanoparticles may be dispersed at a high density byrepeating the immersing (S130), drying (S140) and reducing (S150)processes, thereby improving the conductive percolation network ofstretchable nanofibers 11.

Furthermore, when forming a mat using stretchable nanofibers 11, astretchable conductive mat may be formed by the processes describedabove.

The resulting stretchable conductive nanofibers 10 may be used asfiber-based devices such as wearable displays, wearable solar systems,wearable self powering energy generators, or used in bio health caresuch as E-skin, artificial muscles, or a wearable electrocardiogram(ECG).

Also, the resulting stretchable conductive nanofibers 10 or thestretchable conductive nanofiber mat may be used as a stretchableelectrode.

EXAMPLE 1

(a) Poly (styrene-b-butadiene-b-styrene) (SBS) polymer (Sigma-Aldrich,styrene 21 weight %) was dissolved in a 3:1 (v/v) mixed solution oftetrahydrofuran (THF) and dimethylformamide (DMF) with a 7:3 (SBS 7,solvent 3) weight ratio to prepare a SBS polymer solution. The SBSpolymer solution was electrospinned at 20 a/min of feed rate and 18 kVof applied voltage to produce a SBS nanofiber mat composed of SBSnanofibers.

FIG. 3A is a scanning electron microscope (SEM) image showing the SBSnanofiber mat formed by electrospinning As shown in FIG. 3A, SBSnanofibers were aggregated to form a mat. FIG. 3B is an enlarged imageof a SBS nanofiber in the selected region of FIG. 3A. In FIG. 3B, it canbe seen that the SBS nanofiber has a diameter of about 2.5μum. Thethickness of the resulting SBS nanofiber mat is 200 μm.

(b) Silver trifluoroacetate(STA: AgCF₃COO)(Sigma-Aldrich) was dissolvedin ethanol with an 8:2 ratio (in weight) to prepare a silver precursorsolution.

(c) The SBS nanofiber mat was immersed in the silver trifluoroacetate(STA) solution for 30 minutes. Ethanol dissolves STA as well as swellsSBS nanofibers, so STA may be penetrated into SBS nanofibers of the mat.After the immersion, the SBS nanofiber mat was removed from the silverprecursor solution and dried at room temperature to remove ethanol fromthe SBS nanofiber mat. As a result, a SBS nanofiber mat having STAdispersed therein and deposited on the surface thereof was obtained.

FIG. 4A is a SEM image of a surface of the SBS nanofiber mat after beingimmersed in the STA solution, removed, and dried. FIG. 4B is an enlargedSEM image of a selected region of FIG. 4A. In FIG. 4A and FIG. 4B, itcan be seen that STA particles were also formed on the surface of theSBS nanofibers.

(d) Concentrated hydrazine hydrates ((N₂H₄) (50-60% hydrazine,Sigma-Aldrich)) was dropped on the SBS nanofiber mat removed from asilver precursor solution, and silver trifluoroacetate inside and on thesurface of the SBS nanofibers was reduced. After 5 minutes, the SBSnanofiber mat was rinsed with deionized water several times to removeremaining hydrazine hydrates. As a result, a SBS nanofiber mat havingsilver nanoparticles dispersed therein and deposited on the surfacethereof was obtained.

FIG. 5A is a cross section image of SBS nanofibers of a stretchableconductive SBS nanofiber mat, and FIG. 5B is an transmission electronmicroscopy TEM image of a selected region of FIG. 5A. The dark part ofthe image in FIG. 5B shows silver nanoparticles, and the silvernanoparticles forming a percolation network inside the SBS nanofibersare apparent by their distribution and connection.

Swelling Ratio

FIG. 6 is a graph showing a swelling ratio of a SBS nanofiber matimmersed in a STA solution according to an STA concentration in ethanol.The swelling ratio of the SBS nanofiber mat represents the ratio betweena length of one side of an electrospinned SBS nanofiber mat and thelength of the same side of the SBS nanofiber mat after 30 minutes ofimmersion in the STA solution.

With reference to FIG. 6, in which the graph shown in a smaller boxshows an enlarged curve at concentrations from 1.0 to 2.0 wt % of STA,an increase in the swelling ratio of the SBS nanofiber mat wasinsignificant or unnoticeable when the weight % of STA was between about0 and about 1.5, but the swelling ratio of the SBS nanofiber matincreased rapidly to about 1 through about 1.5 when the weight % of STAwas between about 1.5 and about 2. The swelling ratio of SBS nanofibermat at the weight % of STA between about 2 and about 20 increasedgradually from about 1.5 to about 1.7. When the weight % of STA inethanol was 0, the swelling ratio of the SBS nanofiber mat was almost 1.The fact that the swelling ratio of the SBS nanofiber mat increases asthe weight % of STA increases shows that the swelling of the SBSnanofiber mat is due to STA. In other words, the swelling of the SBSnanofiber mat of SBS nanofibers occurs when STA penetrates inside of ordeposits on the surface of SBS nanofibers.

Fourier Transform Infrared Spectroscopy (FT-IR) Analysis

FIG. 7 is a graph showing FT-IR analysis of a SBS nanofiber mat immersedin a STA solution. The FT-IR analysis was performed after immersing theSBS nanofiber mat in a 15 weight % STA solution, and then removing anddrying it. C-F asymmetrical stretching peaks of STA were found at1128.17 cm⁻¹ and 1182.16 cm⁻¹, and thus, the STA in SBS was confirmed.

Also, thermogravimetry analysis showed 60 wt % of silver content, andsuch a high content of silver was possible due to the silverdistribution inside the SBS nanofibers besides the silver content on thesurface of the SBS nanofibers. It is believed that a high content ofsilver nanoparticles both on the surface and inside the SBS nanofibersenhances a percolation network of silver nanoparticles both inside andoutside the SBS nanofibers. Thus, a conductive SBS nanofiber mat mayhave high conductivity, and thereby reduce significantly the lowering ofconductivity of nanofibers when straining is exerted on the nanofibers.

Strain Test

FIG. 8 is a graph showing surface resistance measurements according tothe number of straining exerted on conductive SBS nanofiber mat.Straining was exerted up to 300 times, and the surface resistance of theconductive SBS nanofiber mat was measured at a strain ratio from 0.2 to1.4 with a period of 0.2. When the strain ratio was low, the sheetresistance was also low, but almost no change was made to the sheetresistance according to the number of straining for each strain ratio.This shows that a percolation network of silver nanoparticles inside theSBS nanofiber mat was stably formed.

FIG. 9A and FIG. 9B are images showing a circuit connection before andafter straining was exerted on the SBS nanofiber mat in a light bulbcircuit using the SBS nanofiber mat as an electrode. FIG. 9A is an imageof a turned-on light bulb before straining was exerted on the electrode,and FIG. 9B is an image of a turned-on light bulb after 60% strain wasexerted on the electrode. From FIG. 9B, it is shown that theconductivity of the SBS nanofiber mat electrode was kept constant at astrain ratio of 0.6.

FIG. 10 is a graph showing a current-voltage characteristic according tothe strain ratio of the conductive SBS nanofiber mat. The specificresistance of the SBS nanofiber mat according to the strain ratio wasobtained from the graph of FIG. 10. The specific resistance of the SBSnanofiber mat was 1.04×10⁻⁶ Ω·m before straining was exerted, and1.96×10⁻⁶ Ω·m at the strain ratio of 0.6 (60% strain) as specificresistance increases when strain ratio increases.

By forming a conductive percolation network inside stretchablenanofibers 11, a strain range while still maintaining conductivity instretchable nanofibers 11 may be increased.

It should be understood that the exemplary embodiments described hereinshould be considered in a descriptive sense only and not for purposes oflimitation. Descriptions of features or aspects within each embodimentshould typically be considered as available for other similar featuresor aspects in other embodiments.

1. A stretchable conductive nanofiber, comprising: a stretchablenanofiber; and a percolation network of conductive nanoparticles formedinside the stretchable nanofibers.
 2. The stretchable conductivecomposite nanofiber of claim 1, wherein the stretchable nanofiber isformed of a polybutadiene, poly(styrene-butadiene),poly(styrene-butadiene-styrene),poly(styrene-ethylene-butylene-styrene), ethylene prolylene dienerubber, acrylic rubber, polychloroprene rubber, polyurethane, florinerubber, butyl rubber, polyisoprene, or a mixture thereof.
 3. Thestretchable conductive composite nanofiber of claim 1, wherein theconductive nanoparticles comprise silver, gold, copper, palladium orplatinum and the average dimension of the conductive nanoparticles. 4.The stretchable conductive composite nanofiber of claim 1, which is in aform of a mat formed of a plurality of the stretchable conductivecomposite nanofibers.
 5. The stretchable conductive composite nanofiberof claim 1, further comprising conductive nanoparticles bound to asurface of the stretchable composite nanofiber.
 6. The stretchableconductive composite nanofiber of claim 5, wherein the total mass of theconductive nanoparticles is in a range of about 30 to about 70 weightpart based on 100 weight part of the total mass of the stretchableconductive composite nanofiber.
 7. A stretchable conductive electrodecomprising stretchable conductive nanofibers according to claim
 1. 8. Astretchable conductive electrode comprising the mat of stretchableconductive nanofibers according to claim
 4. 9. A method of producingstretchable conductive nanofibers, the method comprising: formingstretchable nanofibers; preparing a metal precursor solution bydissolving metal precursors in a solvent that may swell the stretchablenanofibers; immersing the stretchable nanofibers in the metal precursorssolution to swell the stretchable nanofibers, to penetrate and dispersethe metal precursors inside the stretchable nanofibers; removing thestretchable nanofibers from the solution of metal precursors; drying thestretchable nanofibers removed from the solution of metal precursorss;and reducing the metal precursors penetrated inside the stretchablenanofibers to metal nanoparticles.
 10. The method of claim 9, whereinthe stretchable conductive nanofibers are formed by electrospinning. 11.The method of claim 9, wherein the stretchable nanofibers are formed ofpolybutadiene, poly(styrene-butadiene), poly(styrene-butadiene-styrene),poly(styrene-ethylene-butylene-styrene), ethylene prolylene dienerubber, acrylic rubber, polychloroprene rubber, polyurethane, florinerubber, butyl rubber, polyisoprene or a mixture thereof.
 12. The methodof claim 9 wherein the stretchable nanofibers have a diameter in a rangeof about 100 nm to about 5.0 μm.
 13. The method of claim 9, wherein themetal precursors comprise AgNO₃, AgCl, HAuCl₄, CuCl₂, PtCl₂, or PtCl₄.14. The method of claim 9, wherein the solvent of the metal precursorsolution comprises water, methanol, ethanol, propanol, isopropylalcohol, butanol, ethylene glycol, dimethylformamide, tetrahydrofuran ora mixture solvent of more than two thereof.
 15. The method of claim 9,wherein the metal precursor solution comprises the metal precursors in arange of about 30 to about 70 weight %.
 16. The method of claim 9,wherein the reducing metal precursors uses a reducing agent.
 17. Themethod of claim 16, wherein the reducing agent is hydrazine (N₂H₄)vapor, concentrated hydrazine, or a sodium borohydride (NaBH₄) solution.18. The method of claim 12, wherein the metal precursors are depositedon the surface of the stretchable nanofibers during the immersion of thestretchable nanofibers in the metal precursor solution.
 19. The methodof claim 18, wherein the metal precursors deposited on the surface ofthe stretchable nanofibers are also reduced during the reduction of themetal precursors that have penetrated inside the stretchable nanofibersto metals.
 20. The method of claim 12, wherein the stretchablenanofibers form a mat.